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- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion type Assertion NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_head.
- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion description "[Of the 45 patients, 5 (11.1%) showed mutations in the MYBPC3 gene (2 deletions and 3 missense mutations), all in patients with familial HCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_provenance.
- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion evidence source_evidence_literature NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_provenance.
- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion SIO_000772 16566405 NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_provenance.
- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion wasDerivedFrom befree-20140225 NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_provenance.
- NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_assertion wasGeneratedBy ECO_0000203 NP189893.RAyetrRcytPQ2QmYDSNvsCoCh4itzlwSZnzQIqkGkHaco130_provenance.